Saturday, April 01, 2017 3:44:55 PM
you spend none of your time here sharing any of the DD you find with us.
That is true, most of the fruits of my DD lately have not been positive for the company, the management, or the science.
Since this is the second time recently you have criticized my lack of DD, maybe I will discuss something. I thought of posting it a week ago when I first watched the video, but decided against it. Anyway in the video posted on Medscape entitled "Management of Glioblastoma: Where Have We Been and Where Are We Going?" Dr. Prins and Dr. Martin van deb Bent have an interesting discussion about the various recent trials for GBM.
Dr. Bent has some very interesting takeaways from the failed CLDX Rindo trial that I found very interesting. Some of his overall comments were similar to what we heard in December from Dr. Liau. Like early phase trials and patient selection bias for example, and how early positive results from small samples didn't always lead to a favorable outcome in the controlled trial setting. But what I found most interesting were his comments regarding the failed CLDX Rindo trial and how the trial protocol and patient characters led to "everyone living longer" in the trial.
I'm curious if you/flipper watched the video? What parallels (if any) do you see between the ACT IV trial and the L phase 3? Which of Dr. Bent's comments and concerns do you think may be applicable to the L phase 3 trial? Why do you suppose Dr. Prins didn't make more mention of vaccines playing a significant role in the future treatment landscape as a single agent? Why do you suppose there seems to be a marked shift by the doctors heavily involved in the vaccine research at UCLA toward combination trials offering the best avenue for GBM treatment exploration going forward?
Recent NWBO News
- Northwest Biotherapeutics Announces Establishment Of the Company's Own Dedicated Leukapheresis Clinic • PR Newswire (US) • 04/21/2026 01:30:00 PM
- Northwest Biotherapeutics Announces Establishment Of the Company's Own Dedicated Leukapheresis Clinic • PR Newswire (US) • 04/21/2026 01:30:00 PM
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 04/21/2026 04:15:08 AM
- Form POS AM - Post-Effective amendments for registration statement • Edgar (US Regulatory) • 04/16/2026 09:25:30 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 04/07/2026 04:30:50 PM
- Form NT 10-K - Notification of inability to timely file Form 10-K 405, 10-K, 10-KSB 405, 10-KSB, 10-KT, or 10-KT405 • Edgar (US Regulatory) • 03/31/2026 09:04:37 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/15/2026 10:06:20 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 01/02/2026 10:14:59 PM
- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 11/28/2025 09:43:27 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/25/2025 10:23:07 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/20/2025 09:26:03 PM
- Form PRE 14A - Other preliminary proxy statements • Edgar (US Regulatory) • 11/19/2025 09:15:48 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/14/2025 09:44:21 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/31/2025 04:29:10 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/30/2025 08:40:05 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/24/2025 04:28:38 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/14/2025 06:22:26 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/14/2025 09:00:38 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 07/01/2025 09:04:38 PM
